EP2832367B1 - Agent pour prévenir ou traiter une tumeur de cellule géante ou un chondrosarcome survenant dans un os/tissu mou - Google Patents

Agent pour prévenir ou traiter une tumeur de cellule géante ou un chondrosarcome survenant dans un os/tissu mou Download PDF

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EP2832367B1
EP2832367B1 EP13769796.7A EP13769796A EP2832367B1 EP 2832367 B1 EP2832367 B1 EP 2832367B1 EP 13769796 A EP13769796 A EP 13769796A EP 2832367 B1 EP2832367 B1 EP 2832367B1
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pparγ
cells
bone
chondrosarcoma
zaltoprofen
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EP2832367A4 (fr
EP2832367A1 (fr
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Akihiko Takeuchi
Hiroyuki Tsuchiya
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Nippon Chemiphar Co Ltd
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Nippon Chemiphar Co Ltd
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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    • A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
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    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42—Oxazoles
    • A61K31/421—1,3-Oxazoles, e.g. pemoline, trimethadione
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    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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Definitions

  • the present invention relates to a prophylactic or therapeutic agent and the like for giant cell tumors occurring in a bone and soft tissue or for chondrosarcoma, in which agent a non-steroidal anti-inflammatory agent is used.
  • the present invention also relates to a screening method for selecting a substance as a prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or for chondrosarcoma, which substance induces expression of PPAR ⁇ , and thereby induces apoptosis or fat cell differentiation,.
  • Osteoclastoma is a benign tumor frequently occurring in circumferences of the knee joints of young to middle- or advanced-aged persons, and the patients' man-and- woman ratio is 1:1.3 to 1.5, which means higher morbidity of women. Osteoclastoma accounts for about 5% of the total bone tumors, and accounts for about 20% of benign bone tumors. Although it is a benign tumor, the recurrence rate thereof is as high as 10 to 30%, and therapeutic treatment may sometimes be troubled by metastases to lung or malignant transformation. The major pathological finding is hyperplasia of multinucleated giant cells and monocyte cells, and spindle cells are observed among them.
  • the body of the tumor is not these multinucleated giant cells, but fibroblast-like spindle cells present in the stroma. Further, since it occurs in the vicinity of a joint such as knee joint, shoulder joint, and wrist joint, it is important how the recurrence is prevented, and how a treatment is performed with conserving the joint function.
  • Giant cell tumor of tendon sheath is a neoplastic disease occurring from tendon sheath, joint, or synovial membrane of synovial bursa. It is classified into the localized type and diffused type on the basis of the growth type of a lesion, and it is generally considered that a lesion of the localized type is synonymous to the giant cell tumor of tendon sheath, and giant cell tumor of tendon sheath of the diffused type is synonymous to the pigmented villonodular synovitis. Giant cell tumor of tendon sheath frequently occurs in women in their thirties to fifties, and in about 85% of patients, it occurs in the vicinity of joints of fingers or on the flexor tendon, and it secondly frequently occurs in toes.
  • Pigmented villonodular synovitis occurs in relatively young adults not older than 40, and slightly more frequently occurs in women. It most frequently occurs in the knee joint, and also occurs in the hip, leg, elbow, shoulder joints, and the like. Villus images and tubercle-like proliferation of the synovial membrane are caused in the joints, and hemarthrosis is often observed. Since it may infiltrate into bones, secondary osteoarthritis may occur. As the pathological findings, there are intermingled synovial cell-like monocytes, multinucleated giant cells, foam cells, siderophores, inflammatory cells, and the like. As the therapeutic treatment, the tumor is surgically resected, but total resection is difficult, and therefore the recurrence rate is as high as 40 to 50%.
  • any effective therapies have not been developed at present, except for surgical operation.
  • Chondrosarcoma accounts for about 20% of primary malignant bone tumors, and shows the secondly highest occurrence frequency following that of bone sarcoma. It is histologically classified into conventional chondrosarcoma, periosteal chondrosarcoma, mesenchymal chondrosarcoma, dedifferentiated chondrosarcoma, clear-cell chondrosarcoma, extraskeletal myxoid chondrosarcoma, and the like. Typical chondrosarcoma frequently occurs in thirties to fifties, and slightly more frequently occurs in men.
  • chondrosarcoma is a non-cartilaginous highly malignant tumor developed from a low malignancy conventional chondrosarcoma, and they are developed in contiguity with each other, but with a definite boundary.
  • chondrosarcoma frequently occurs in persons in their twenties to fifties, and in about 2/3 of the patients, it occurs in humeral head or femoral head. It also occurs in cranical bone, spine, and bones of hand and foot. Extraskeletal myxoid chondrosarcoma frequently occurs in persons in their forties and fifties, and may occur in deep part soft tissues of proximal parts of extremities such as thigh, and of the truncus, and soft tissues such as end parts of extremities, mediastinum and retroperitoneum. For these types of chondrosarcoma, any effective therapies have not been developed so far, except for surgical operation.
  • the peroxisome proliferator-activated receptor ⁇ (PPAR ⁇ ) is a protein belonging to the intranuclear receptor superfamily, and also functions as a transcription factor. Although PPAR ⁇ is mainly distributed over fat tissues, and participates in fat cell differentiation and the like, expression thereof is also observed in macrophages, vascular endothelial cells and the like. As the other activities thereof, it has been reported that the protein has an antidiabetic activity, anti-arteriosclerotic activity, bone metabolism related activity, antitumor activity, and anti-inflammatory activity.
  • Non-patent documents 1 and 2 it has been reported that activation of PPAR ⁇ induces apoptosis in various tumors (Non-patent documents 1 and 2), and expression of PPAR ⁇ has been confirmed in various cancer cells, such as cells of breast cancer (Non-patent document 3), colon cancer (Non-patent document 4), or lung cancer (Non-patent document 5). Moreover, it has been reported that activation of PPAR ⁇ is also induced by a non-steroidal anti-inflammatory agent besides a PPAR ⁇ ligand, resulting induction of cell death (Non-patent document 6).
  • Patent document 1 WO2008/026729
  • An object of the present invention is to provide a substance that induces expression of PPAR ⁇ in giant cell tumor occurring in a bone and soft tissue or that in chondrosarcoma, and induces apoptosis or fat cell differentiation mediated by PPAR ⁇ as a prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or for chondrosarcoma.
  • Another object of the present invention is to provide a screening method for selecting a substance as a prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or for chondrosarcoma, which substance induces expression of PPAR ⁇ , and thereby induces apoptosis or fat cell differentiation.
  • PPAR ⁇ was not usually expressed in giant cell tumor occurring in a bone and soft tissue or chondrosarcoma. Whilst they also observed that PPAR ⁇ was expressed in osteoclastoma, which is giant cell tumor occurring in a bone and soft tissue, in a patient administered with zaltoprofen which is one of non-steroidal anti-inflammatory agents and has a PPAR ⁇ -agonistic activity, and that apoptosis or differentiation into fat cells were induced.
  • the inventors of the present invention further conducted researches on the basis of the aforementioned findings, and as a result, accomplished the present invention.
  • the present invention thus provides a pharmaceutical composition according to claim 1.
  • Preferred embodiments of the invention are set out in claims 2 to 4.
  • the prophylactic or therapeutic agent of the present invention can be administered to a patient with giant cell tumor occurring in a bone and soft tissue or with chondrosarcoma as a chemotherapeutic drug to be administered before or after a surgical operation, or it can be administered to a person having a risk of onset of giant cell tumor occurring in a bone and soft tissue or that of chondrosarcoma as a prophylactic agent.
  • a test substance that controls PPAR ⁇ and apoptosis or fat cell differentiation it becomes possible to retrieve a novel prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or for chondrosarcoma.
  • the inventors of the present invention found that PPAR ⁇ was not expressed in cells derived from patients with giant cell tumor occurring in a bone and soft tissue, and they also found that a specific substance having a PPAR ⁇ -agonistic activity induced expression of PPAR ⁇ in giant cell tumor occurring in a bone and soft tissue, and simultaneously induced apoptosis or fat cell differentiation. Therefore, the present invention provides a prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue, which can induce apoptosis or fat cell differentiation mediated by PPAR ⁇ in giant cell tumor occurring in a bone and soft tissue on the basis of the PPAR ⁇ expression-inducing activity and the PPAR ⁇ -agonistic activity.
  • the present invention also provides a prophylactic or therapeutic agent for chondrosarcoma, which can induce apoptosis or fat cell differentiation mediated by PPAR ⁇ on the basis of the PPAR ⁇ expression-inducing activity and the PPAR ⁇ -agonistic activity.
  • the giant cell tumor occurring in a bone and soft tissue to which the prophylactic or therapeutic agent of the present invention can be applied is not particularly limited, so far as giant cells developed in a bone and soft tissue are observed in the tumor.
  • the agent of the present invention can be preferably applied to a tumor that generates giant cells in circumferences of bone, joint, or tendon sheath.
  • the tumor in which giant cells developed in a bone and soft tissue are observed is preferably a benign tumor.
  • Examples of such a tumor include, for example, osteoclastoma, giant cell tumor of tendon sheath, pigmented villonodular synovitis, and the like.
  • benign giant cell tumor occurring in a bone and soft tissue also include chondroblastoma, nonossifying fibroma, osteoblastoma, aneurysmal bone cyst, and the like.
  • chondrosarcoma examples include conventional chondrosarcoma, periosteal chondrosarcoma, mesenchymal chondrosarcoma, dedifferentiated chondrosarcoma, clear-cell chondrosarcoma, extraskeletal myxoid chondrosarcoma, and the like.
  • the prophylactic or therapeutic agent of the present invention can also be used for a tumor in which expression of PPAR ⁇ is observed.
  • a tumor in which expression of PPAR ⁇ is observed include breast cancer, colon cancer, lung cancer, thyroid gland cancer, esophageal cancer, gastric cancer, pancreatic cancer, liver cancer, kidney cancer, vesical cancer, ovarian cancer, uterine cervix carcinoma, prostate cancer, malignant melanoma, leukemia, malignant lymphoma, liposarcoma, leiomyosarcoma, bone sarcoma, and the like.
  • PPARy is a protein belonging to the intranuclear receptor superfamily, and it recognizes the PPAR response element (PPRE) when it has formed a heterodimer with the retinoid X receptor (RXR), which is one of the intranuclear receptors, and activates transcription of a gene downstream therefrom.
  • PPRE PPAR response element
  • RXR retinoid X receptor
  • examples of such a substance having a PPAR ⁇ expression-inducing activity and a PPAR ⁇ -agonistic activity include non-steroidal anti-inflammatory agents. Therefore, the prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or chondrosarcoma that can induce apoptosis or fat cell differentiation mediated by PPAR ⁇ in giant cell tumors occurring in a bone and soft tissue or in chondrosarcoma on the basis of a PPAR ⁇ expression-inducing activity and a PPAR ⁇ -agonistic activity is, according to an embodiment of the present invention, a prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or for chondrosarcoma, which comprises a non-steroidal anti-inflammatory agent as an active ingredient.
  • the non-steroidal anti-inflammatory agent referred herein is zaltoprofen.
  • the PPAR ⁇ expression-inducing activity of the substances having a PPAR ⁇ expression-inducing activity and a PPAR ⁇ -agonistic activity, which substances include non-steroidal anti-inflammatory agents, can be confirmed by the known methods described later.
  • expression thereof can be confirmed by a method of extracting mRNA from giant cell tumors occurring in a bone and soft tissue or from chondrosarcoma by an ordinary method, and performing a reverse transcription reaction and PCR using primers that enables amplification of a PPAR ⁇ transcription product, or a method of fixing giant cell tumors occurring in a bone and soft tissue or fixing chondrosarcoma, or extracting a cell disruption product, and confirming expression of a PPAR ⁇ translation product by using an antigen-antibody reaction using antibodies directed to the PPAR ⁇ translation product.
  • the transcription product and translation product of PPAR ⁇ are known.
  • nucleotide sequence information is disclosed as GenBank accession No.
  • the PPAR ⁇ -agonistic activity can be confirmed by, for example, measuring expression level of a downstream gene, or expression level of a lipid.
  • the gene locating downstream of PPAR ⁇ include, for example, an apoptosis-related gene, fat cell differentiation-related gene, arteriosclerosis-related gene, anti-inflammation-related gene, and the like.
  • the apoptosis-related gene may be a gene responsible for an apoptosis signal, or may be a marker gene for apoptosis.
  • Examples of the apoptosis-related gene include, for example, those of caspase 3, p53, and the like.
  • nucleotide sequence information is disclosed as GenBank accession No. BC016926, and as for the translation product thereof, amino acid sequence information is disclosed as GenBank accession No. AAH16926.
  • nucleotide sequence information is disclosed as GenBank accession No. NM_000546, and as for the translation product thereof, amino acid sequence information is disclosed as GenBank accession No. NP_000537.
  • the fat cell differentiation-related gene may be a gene that induces differentiation into fat cells, or may be a marker gene for fat cell differentiation.
  • Examples of the fat cell differentiation-related gene include, for example, those of Setd8 (SET domain containing (lysine methyltransferase) 8), Setdb1 (SET domain, bifurcated 1), LPL (Lipoprotein Lipase), leptin, FABP4/aP2 (fatty acid-binding protein-4), adiponectin, a2Col6 (a chain 2 of type 6 collagen), and the like.
  • Setd8 SET domain containing (lysine methyltransferase) 8
  • Setdb1 Setdb1
  • LPL Lipoprotein Lipase
  • leptin leptin
  • FABP4/aP2 fatty acid-binding protein-4
  • adiponectin a2Col6 (a chain 2 of type 6 collagen)
  • a2Col6 a chain 2 of type 6 collagen
  • nucleotide sequence information is disclosed as GenBank accession No. BC028671, and as for the translation product thereof, amino acid sequence information is disclosed as GenBank accession No. AAH28671.
  • amino acid sequence information is disclosed as GenBank accession No. AAH11353.
  • nucleotide sequence information is disclosed as GenBank accession No. BC069452, and as for the translation product thereof, amino acid sequence information is disclosed as GenBank accession No. AAH69452.
  • nucleotide sequence information is disclosed as GenBank accession No. BC003672, and as for the translation product thereof, amino acid sequence information is disclosed as GenBank accession No. AAH03672.
  • nucleotide sequence information is disclosed as GenBank accession No. BC096308, and as for the translation product thereof, amino acid sequence information is disclosed as GenBank accession No. AAH96308.
  • nucleotide sequence information is disclosed as GenBank accession No. BC002483, and as for the translation product thereof, amino acid sequence information is disclosed as GenBank accession No. AAH002483.
  • arteriosclerosis-related gene examples include, for example, those of AT1R (angiotensin II receptor I), and the like.
  • AT1R angiotensin II receptor I
  • nucleotide sequence information is disclosed as GenBank accession No. BC068494
  • amino acid sequence information is disclosed as GenBank accession No. AAH68494.
  • anti-inflammation-related gene examples include, for example, those of NF- ⁇ B (nuclear factor kappa-light-chain-enhancer of activated B cells), and the like.
  • NF- ⁇ B nucleotide sequence information is disclosed as GenBank accession No.
  • the lipid is not particularly limited so long as it is a lipid contained in fat cells or tissues, and examples include phospholipids, glycolipids, lipoproteins, acylglycerols, ceramides, and the like.
  • the PPAR ⁇ expression-inducing activity can be examined by preparing an RNA (for example, total RNA, or mRNA) fraction from a cell, and detecting the transcription product of the PPAR ⁇ gene contained in the fraction.
  • an RNA fraction can be prepared by a known method such as the guanidine-CsCl ultracentrifugation method and the AGPC method, and total RNA of high purity can be quickly and conveniently prepared from a small number of cells by using a commercial kit for RNA extraction (for example, RNeasy Mini Kit produced by QIAGEN and the like).
  • Examples of the means for detecting a transcription product of a gene in an RNA fraction include, for example, a method of using hybridization (Northern blotting, dot blotting, DNA chip analysis, and the like), a method of using PCR (RT-PCR, competitive PCR, real-time PCR, and the like), and the like.
  • the quantitative PCR method as competitive PCR and real-time PCR is preferred, since it enables quick and convenient detection of change of expression of a gene from an extremely small amount of sample with good quantification ability.
  • the PPAR ⁇ gene can be detected by, for example, using a nucleic acid probe that enables specific detection of a transcription product of the gene.
  • the nucleic acid probe used for measurement of the PPAR ⁇ expression-inducing activity is a polynucleotide comprising a contiguous part or all of the gene containing about 15 or more nucleotides, preferably about 18 to 500 nucleotides, more preferably about 18 to 200 nucleotides, still more preferably about 18 to 50 nucleotides, or a polynucleotide comprising a complementary sequence thereof.
  • the polynucleotide may be either DNA or RNA, or may be a DNA/RNA chimera. Preferably the polynucleotide includes DNA. Further, the polynucleotide used as the probe may be a double-stranded or single-stranded polynucleotide. The double-stranded polynucleotide may be a double-stranded DNA, double-stranded RNA, or a hybrid of DNA and RNA. In the case of the single-stranded polynucleotide, an antisense strand can be used.
  • the nucleic acid probe used for the measurement of the PPAR ⁇ expression-inducing activity is a polynucleotide containing a nucleotide sequence that can hybridize with a transcription product of the PPAR ⁇ gene under stringent conditions.
  • the hybridization can be performed by a method known per se or a method similar to such a known method, for example, the methods described in Molecular Cloning, 2nd edition (J. Sambrook et al., Cold Spring Harbor Lab. Press, 1989 ), and the like.
  • Examples of the stringent conditions include, for example, a hybridization reaction at 45°C in 6 x SSC (sodium chloride/sodium citrate) followed by once or more times of washing in 0.2 x SSC/0.1% SDS at 65°C, and the like.
  • Those skilled in the art can adjust the stringency to be a desired stringency by appropriately changing salt concentration of the hybridization solution, temperature for the hybridization reaction, concentration of the probe, length of the probe, number of mismatches, time of the hybridization reaction, salt concentration of the washing solution, temperature for washing, and the like.
  • the nucleic acid that functions as a probe capable of detecting expression of the PPAR ⁇ gene can be obtained by amplifying a nucleic acid of a desired length by PCR using a primer set that is capable of amplifying a part or all of a transcription product of the gene, and as the template, cDNA or genomic DNA derived from any of cells [for example, hepatic cells, splenic cells, nerve cells, glia cells, pancreatic 6 cells, marrow cells, mesangial cells, Langerhans cells, epidermal cells, epithelial cells, goblet cells, endothelial cells, smooth muscle cells, fibroblasts, fibrocytes, myocytes, fat cells, immunocytes (for example, macrophage, T cell, B cell, natural killer cell, mast cell, neutrophile, basophile, eosinophile, monocyte), megakaryocytes, synovial cells, chondrocytes, osteocytes, osteoblasts, osteoclasts
  • nucleic acid that functions as a primer that is capable of amplifying a part or all of the transcription product of the PPAR ⁇ gene can be obtained by chemical synthesis of a part of the nucleotide sequence and a complementary strand sequence thereof based on the nucleotide sequence information of the aforementioned PPARy gene, using a commercial automatic DNA/RNA synthesizer.
  • the nucleic acid is preferably labeled with a labeling agent, in order to make it possible to detect and quantify the target nucleic acid.
  • a labeling agent for example, a radioactive isotope, enzyme, fluorescent substance, luminescent substance, and the like are used.
  • the radioactive isotope for example, [ 32 P], [ 3 H], [ 14 C], and the like are used.
  • the enzyme a stable enzyme showing a high specific activity is preferred, and there are used, for example, ⁇ -galactosidase, ⁇ -glucosidase, alkaline phosphatase, peroxidase, malate dehydrogenase, and the like.
  • fluorescent substance for example, fluorescamine, fluorescein isothiocyanate, and the like are used.
  • luminescent substance for example, luminol, luminol derivatives, luciferin, lucigenin, and the like are used.
  • biotin-(strept)avidin can be used for the binding of the probe and the labeling agent.
  • RNA fraction prepared as described above to separation by gel electrophoresis, blotting RNA to a membrane such as cellulose nitrate, nylon, or polyvinylidene difluoride membrane, allowing specific hybridization in a hybridization buffer containing a labeled probe prepared as described above, and then measuring amount of the labeling agent binding to the membrane for each band by an appropriate method, expression amount of the PPARy gene can be measured.
  • dot blotting by similarly allowing a hybridization reaction of the RNA fraction spotted on a membrane, and measuring amount of the labeling agent for each spot, expression amount of the gene can be measured.
  • cDNA introduced with an appropriate promoter such as T7 promoter is synthesized from the RNA fraction prepared as described above by a reverse transcription reaction, and cRNA is further synthesized by using an RNA polymerase (if a mononucleotide labeled with biotin or the like is used as a substrate in this synthesis, a labeled cRNA can be obtained).
  • RNA polymerase if a mononucleotide labeled with biotin or the like is used as a substrate in this synthesis, a labeled cRNA can be obtained.
  • the quantitative PCR method is used as the method for measuring expression amount of the PPAR ⁇ gene.
  • the quantitative PCR for example, competitive PCR, real-time PCR, and the like are available.
  • examples of the set of oligonucleotides used as primers in PCR include, for example, nucleic acid primers that enable specific detection of a transcription product of the aforementioned PPAR ⁇ gene.
  • examples include a set of oligonucleotides comprising a polynucleotide complementary to a polynucleotide (sense strand) sequence having a length of a contiguous nucleotide sequence containing about 15 or more nucleotides, preferably about 15 to 50 nucleotides, more preferably about 15 to 30 nucleotides, still more preferably about 15 to 25 nucleotides, and designed so that it can amplify a DNA fragment of about 100 bp to several kbp, and a polynucleotide that can hybridize with a polynucleotide (antisense strand) having a nucleotide sequence complementary
  • the competitive RT-PCR means a method of calculating amount of an objective DNA by competitively performing amplification reactions in a reaction mixture also containing, as a competitor, a known amount of another template nucleic acid which can be amplified with a set of primers that can amplify the objective DNA, and comparing amounts of amplified products.
  • the competitive RT-PCR when used, there is used a known amount of a competitor nucleic acid that can be amplified with the aforementioned primer set, of which amplification product can be distinguished (on the basis of, for example, difference of amplified sizes, difference of migration patterns of restriction enzyme-processed fragments observed in electrophoresis, and the like) from the amplification product of the target nucleic acid (namely, transcription product of the nucleotide sequence information on the PPAR ⁇ gene) after the amplification, in addition to the aforementioned primer set.
  • the target nucleic acid and the competitor nucleic acid are competitively amplified, since they use the same primers, and therefore the ratio of the amounts of the amplification products reflects the ratio of the amounts of the original templates.
  • the competitor nucleic acid may be DNA or RNA.
  • the competitor nucleic acid is DNA
  • cDNA is synthesized by a reverse transcription reaction from an RNA fraction prepared as described above
  • PCR can be performed in the presence of the aforementioned primer set and the competitor.
  • the competitor is RNA
  • the competitor is added to an RNA fraction to perform a reverse transcription reaction
  • the aforementioned primer set can be added to perform PCR. In the latter case, efficiency of the reverse transcription reaction is also taken into consideration, and therefore the absolute amount of the original mRNA can be estimated.
  • the real-time PCR is a method of monitoring amount of amplification product in real time by using a fluorescent reagent, and requires an apparatus integrally comprising a thermal cycler and a spectrophotofluorometer. Such an apparatus is marketed.
  • a fluorescent reagent such as, for example, the intercalator method, TaqManTM probe method, Molecular Beacon method, and the like.
  • the aforementioned primer set SYBR Green I
  • a reagent that emits fluorescence when it binds with a double-stranded DNA such as ethidium bromide
  • a fluorescent regent probe
  • the nucleic acid can hybridize to a target nucleic acid in a region to be amplified
  • each end is modified with a fluorescent substance (for example, FAM, HEX, TET, FITC, and the like) or a quenching substance (for example, TAMRA, DABCYL, and the like), e.g.
  • TaqManTM probe or Molecular Beacon probe are added to a reaction system for PCR. Since the intercalator emits fluorescence when it binds with a synthesized double-stranded DNA and irradiated with an excitation light, production amount of the amplification product can be monitored by measuring fluorescence intensity, and the amount of the original template cDNA can be thereby estimated.
  • the TaqManTM probe is an oligonucleotide that can hybridize with the region of the target nucleic acid to be amplified, of which each end is modified with a fluorescent substance or a quenching substance.
  • the Molecular Beacon probe is an oligonucleotide that can hybridize with a region of a target nucleic acid to be amplified and can have a hairpin secondary structure, of which both ends are modified with a fluorescent substance and a quenching substance, respectively.
  • the hairpin secondary structure When it has the hairpin secondary structure, it does not emit fluorescence because of the presence of the quenching substance, but when it hybridizes with a target nucleic acid at the time of annealing, and thus the distance between the fluorescent substance and the quenching substance increases, it emits fluorescence. Therefore, by measuring the fluorescence intensity, production amount of the amplification product can be monitored, and amount of the original template cDNA can be estimated therefrom. Since the real-time RT-PCR enables real time monitoring of the amount of the product amplified in PCR, it does not require electrophoresis, and thus enables quicker analysis of expression of the PPAR ⁇ gene.
  • PPAR ⁇ expression of the PPAR ⁇ gene in a cell can be investigated by preparing a protein fraction from the cell and detecting a translation product of the gene (namely, PPAR ⁇ ) contained in the fraction.
  • PPAR ⁇ can be detected by an immunoassay (for example, ELISA, FIA, RIA, Western blotting, and the like) using antibodies that specifically recognize the protein, or it can be detected by measuring the activity of the protein using a known method.
  • the protein can also be detected by using mass spectrometry such as MALDI-TOFMS.
  • the antibody that specifically recognizes PPAR ⁇ can be prepared by a general available production method using a polypeptide constituting the protein, total sequence of a partial peptide of the polypeptide showing antigenicity, or a partial peptide thereof corresponding to an epitope as an immunogen.
  • examples of the antibody include naturally occurring antibodies such as polyclonal antibodies and monoclonal antibodies (mAb), chimeric antibodies that can be produced by using a gene recombination technique, humanized antibodies, single strand antibodies, and bindable fragments thereof, but not limited to these examples.
  • the antibody is preferably a polyclonal antibody, monoclonal antibodies, or a bindable fragment thereof.
  • the bindable fragment means a partial region of any of the aforementioned antibodies having a specific binding activity, and specific examples thereof include, for example, F(ab') 2 , Fab', Fab, Fv, sFv, dsFv, sdAb, and the like ( Exp. Opin. Ther. Patents, Vol. 6, No. 5, pp.441-456, 1996 ).
  • a class of the antibody is not particularly limited, and the antibody may be any of those having any of isotypes such as IgG, IgM, IgA, IgD, or IgE.
  • the antibody is preferably IgG or IgM, and it is more preferably IgG, if easiness of purification and the like are taken into consideration.
  • the PPAR ⁇ -agonistic activity can be measured in the same manner as that for the measurement of the PPAR ⁇ expression-inducing activity mentioned above, i.e., by preparing an RNA fraction, a protein fraction, or a lipid fraction from a cell, and detecting a transcription product, or a translation product of a gene locating downstream of the PPAR ⁇ gene (for example, apoptosis-related gene, fat cell differentiation-related gene, arteriosclerosis-related gene, anti-inflammation-related gene, and the like) or a lipid contained in the fraction.
  • apoptosis-related gene for example, apoptosis-related gene, fat cell differentiation-related gene, arteriosclerosis-related gene, anti-inflammation-related gene, and the like
  • the methods for preparing the RNA fraction and the protein fraction and the methods for detecting them may be the same as the aforementioned methods explained for the measurement of the PPAR ⁇ expression-inducing activity.
  • the preparation method of a lipid it may be prepared by using a known method, and there can be used, for example, the Folch method in which a lipid is extracted from a sample containing the lipid by adding several-fold volume of a solvent such as a mixture of chloroform and methanol to the sample, the Bligh-Dyer method in which a lipid is extracted by adding several-fold volume of a solvent such as a mixture of chloroform, methanol and water, or the like.
  • the method for detecting the separated lipid it can be detected by using a known method such as liquid chromatography (LC), gas chromatography (GC), and high performance liquid chromatography (HPLC).
  • a method of directly detecting a lipid contained in a fat cell or tissue may also be used.
  • the reagents and the like usable for such a method are marketed, and for example, HCS LipidTOX Phospholipidosis and Steatosis Detection Kit (Invitrogen) and the like can be used.
  • Examples of person to whom the prophylactic or therapeutic agent of the present invention for giant cell tumors occurring in a bone and soft tissue or for chondrosarcoma can be applied, which agent comprises a substance having a PPAR ⁇ expression-inducing activity and has a PPAR ⁇ -agonistic activity used in the present invention as an active ingredient, include, for example, a person who has clinically diagnosed to have giant cell tumor occurring in a bone and soft tissue or have chondrosarcoma, a person suspected to be that mentioned above, and a person for whom onset of such a disease as mentioned above is expected.
  • the therapeutic agent of the present invention can also be preferably applied to a metastatic cancer of which primary lesion is giant cell tumors occurring in a bone and soft tissue or chondrosarcoma.
  • metastatic cancer include those of lung cancer, colon cancer, breast cancer, prostate cancer, esophageal cancer, gastric cancer, liver cancer, biliary carcinoma, spleen carcinoma, renal carcinoma, vesical cancer, uterine cancer, ovarian cancer, testis cancer, thyroid gland cancer, pancreatic cancer, brain tumor, blood tumor, and the like.
  • the prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or for chondrosarcoma of the present invention can be orally used in the form of a tablet, which may have a sugar coating as required, capsule, elixir, microcapsule, or the like, or can be parenterally used in the form of an injection such as a sterile solution or suspension in water or another pharmacologically acceptable solvent.
  • the prophylactic or therapeutic agent can be prepared by forming a mixture together with physiologically acceptable carrier, flavoring agent, excipient, vehicle, preservative, stabilizer, binder, and the like in the form of a generally acceptable unit dosage form required for implementation of pharmaceutical preparation. Amount of the active ingredient in such a preparation as mentioned above is appropriately chosen by taking a dose into consideration, which will be described later.
  • additives that can be mixed in tablets, capsules, and the like, there are used, for example, binders such as gelatin, cornstarch, tragacanth, and gum arabic, excipients such as crystalline cellulose, bulking agents such as cornstarch, gelatin, and alginic acid, lubricants such as magnesium stearate, sweeteners such as sucrose, lactose, and saccharin, flavoring agents such as peppermint, Gaultheria adenothrix oil, and cherry, and the like.
  • binders such as gelatin, cornstarch, tragacanth, and gum arabic
  • excipients such as crystalline cellulose
  • bulking agents such as cornstarch, gelatin, and alginic acid
  • lubricants such as magnesium stearate
  • sweeteners such as sucrose, lactose, and saccharin
  • flavoring agents such as peppermint, Gaultheria adenothrix oil, and cherry, and the like.
  • a sterilized composition used for injection can be formulated by a common pharmaceutical manufacturing method, such as a method of allowing the active ingredient to exist in a vehicle such as a distilled water for injection, or a method of dissolving or suspending the active ingredient in a naturally produced vegetable oil such as sesame oil and coconut oil.
  • a common pharmaceutical manufacturing method such as a method of allowing the active ingredient to exist in a vehicle such as a distilled water for injection, or a method of dissolving or suspending the active ingredient in a naturally produced vegetable oil such as sesame oil and coconut oil.
  • an aqueous solution used for injection examples include physiological saline, an isotonic solution comprising glucose or other auxiliary agents (for example, D-sorbitol, D-mannitol, sodium chloride, and the like), and the like.
  • aqueous solution may also be used in combination with appropriate solubilizing aids including alcohols (for example, ethanol, and the like), polyalcohols (for example, propylene glycol, polyethylene glycol, and the like), or nonionic surfactants (for example, Polysorbate 80TM, HCO-50, and the like).
  • oily liquid examples include sesame oil and soybean oil, and such oily liquid may be used in combination with a solubilizing aid such as benzyl benzoate or benzyl alcohol.
  • a buffer for example, phosphate buffer, sodium acetate buffer, and the like
  • soothing agent for example, benzalkonium chloride, procaine hydrochloride, and the like
  • stabilizer for example, human serum albumin, polyethylene glycol, and the like
  • preservative for example, benzyl alcohol, phenol, and the like
  • antioxidant antioxidant, and the like
  • the pharmaceutical preparation obtained as described above is safe with reduced toxicity, and therefore it can be administered to, for example, mammals (for example, human, rat, mouse, guinea pig, rabbit, ovine, swine, bovine, equine, cat, dog, ape, and the like).
  • mammals for example, human, rat, mouse, guinea pig, rabbit, ovine, swine, bovine, equine, cat, dog, ape, and the like.
  • a dose of the prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or for chondrosarcoma may differ depending on severity of the giant cell tumor occurring in a bone and soft tissue or that of chondrosarcoma, an object of administration, an administration route and the like
  • the dose may be, for example, in the case of oral administration, generally about 0.1 to 100 mg, preferably about 1.0 to 50 mg, more preferably about 1.0 to 20 mg, per day for an adult (body weight, 60 kg).
  • the dose of the prophylactic or therapeutic agent may also differ depending on an object of administration, severity, and the like.
  • the dose may be, for example, about 0.01 to 30 mg, preferably about 0.1 to 20 mg, more preferably about 0.1 to 10 mg, per day.
  • the object of the administration is an animal, not a human, the agent can be administered at a dose determined from a dose per unit body weight calculated from the aforementioned dose per 60 kg of body weight.
  • the mainstream of the method for therapeutic treatment of osteoclastoma has been extraction of lesion by a surgical operation, and the therapeutic treatment is performed by curetting the tumor in a lesion, and filling a bone lacking part with an allogeneic bone, autogenous bone or artificial bone.
  • a method results in high recurrence rate of the tumor, and suffers from risks of metastasis or malignant transformation in the process of repetition of recurrence.
  • the present invention provides an artificial bone containing a substance having a PPAR ⁇ expression-inducing activity and a PPAR ⁇ -agonistic activity.
  • the substance having a PPAR ⁇ expression-inducing activity and a PPAR ⁇ -agonistic activity contained in the artificial bone of the present invention those mentioned above can be used.
  • Examples of the material used for the artificial bone of the present invention include known biomaterials for orthopedic surgery, for example, metallic materials, ceramic materials, polymer materials, protein materials, and composite materials of these.
  • Examples of the aforementioned metallic substances include, for example, titanium, titanium alloy, stainless steel, cobalt-chrome alloy, and the like.
  • Examples of the aforementioned ceramic materials include, for example, bio-inert ceramics such as alumina ceramics, single crystal alumina ceramics, and zirconia ceramics, and bio-active ceramics such as bioglass ( Hench et al., Biomed. Master. Symp., 2, 117 (1972 )), hydroxyapatite ( Aoki et al., Ceramics, 10, 469 (1975 )), apatite-wollastonite (AW) glass ( Bull. Inst. Chem. Res. KyotoUni., 60, 260 (1982 )), and TCP ceramics (Ca 3 (PO 4 ) 2 ).
  • bioglass Hench et al., Biomed. Master. Symp., 2, 117 (1972 )
  • hydroxyapatite Aoki et al., Ceramics, 10, 469 (1975 )
  • AW apatite-wollastonite
  • poly(methyl methacrylate) PMMA
  • HDP high density polyethylene
  • silicone rubber Teflon
  • polyester polylactic acid
  • PVA hydrogel poly(vinyl) hydrogel
  • Examples of the aforementioned protein materials include, for example, collagen, fibrin, chitin, chitosan, and the like.
  • Ratio of the substance having a PPAR ⁇ expression-inducing activity and having a PPAR ⁇ -agonistic activity in the artificial bone of the present invention consisting of a mixture of the substance having a PPAR ⁇ expression-inducing activity and having a PPAR ⁇ -agonistic activity and an artificial bone material, or an artificial bone material coated with the substance is about 1 to 20%, preferably about 15 to 20%.
  • the inventors of the present invention found that a specific compound having a PPAR ⁇ -agonistic activity induced expression of PPAR ⁇ in giant cell tumors occurring in a bone and soft tissue or chondrosarcoma, and simultaneously induced apoptosis or fat cell differentiation. Therefore, the present invention also provides a method of screening a prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or chondrosarcoma.
  • the method of screening a prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or chondrosarcoma of the present invention comprises the following steps:
  • the cell derived from giant cell tumors occurring in a bone and soft tissue or chondrosarcoma used in the screening method of the present invention may be a primary cultured cell derived from a patient clinically diagnosed to have giant cell tumor occurring in a bone and soft tissue or chondrosarcoma, or a cell of an already established cell line.
  • a cell line can be established according to a method ordinarily performed in this field, or according to a description of published references.
  • the cell derived from giant cell tumors occurring in a bone and soft tissue or from chondrosarcoma may consist of an arbitrary tissue (for example, synovial membrane, joint, cartilage, and the like) containing the cells, and such tissue, organ, or the like may be isolated from a living body and cultured. After a test substance is administered to a living body per se, a biosample may be isolated after a certain period of time.
  • the cell derived from giant cell tumors occurring in a bone and soft tissue or from chondrosarcoma is a cultured cell
  • the cell is cultured in the presence or absence of a test substance.
  • the test substance is not particularly limited, and there are used, for example, a peptide, protein, non-peptide compound, synthetic compound, fermentation product, cell extract, plant extract, animal tissue extract, or the like is used, and these compounds may be novel compounds or known compounds. It is preferred and expected that the test substance is a substance having a PPAR ⁇ expression-inducing activity and having a PPAR ⁇ -agonistic activity. Examples of such test substance include non-steroidal anti-inflammatory agents. Examples of the non-steroidal anti-inflammatory agents include zaltoprofen, diclofenac, indomethacin, and the like as mentioned above.
  • the culture can be performed on an appropriate cell culture base material, and examples of the base material include, for example, flask, flask for tissue culture, dish, petri dish, dish for tissue culture, multidish, microplate, microwell plate, multiplate, multiwell plate, chamber slide, petri dish, tube, tray, culture bag, and roller bottle.
  • Cells derived from giant cell tumors occurring in a bone and soft tissue or chondrosarcoma and suspended as monocells can be suspended in a medium, and inoculated on the aforementioned cell culture base material.
  • the cells are usually cultured in an incubator maintained at 5% CO 2 /95% air and 37°C until the cells reach confluent.
  • a test substance and the cells can be contacted by, for example, contacting a medium suitable for apoptosis of the cells (for example, minimum essential medium (MEM), Dulbecco's modified Eagle's medium (DMEM), RPMI1640 medium, 199 medium, F12 medium, and the like containing about 5 to 20% of fetal bovine serum (FBS)) and any of various buffers (for example, HEPES buffer, phosphate buffer, phosphate buffered saline, Tris-HCl buffer, borate buffer, acetate buffer, and the like) containing the test substance with the cells for a certain period of time.
  • a medium suitable for apoptosis of the cells for example, minimum essential medium (MEM), Dulbecco's modified Eagle's medium (DMEM), RPMI1640 medium, 199 medium, F12 medium, and the like containing about 5 to 20% of fetal bovine serum (FBS)
  • FBS fetal bovine serum
  • concentration of the test substance to be added should be changed depending on the type of the compound (solubility, toxicity, and the like), the concentration is appropriately chosen to be in the range of, for example, about 1 to 1000 ⁇ M, preferably about 5 to 500 ⁇ M, more preferably about 50 to 200 ⁇ M.
  • Time of the contact is, for example, about 1 to 48 hours, preferably about 5 to 36 hours, more preferably about 10 to 24 hours.
  • a test substance and the cells can be contacted for a certain period of time, for example, by adding the test substance in a serum free medium suitable for fat cell differentiation of the cells (for example, minimum essential medium (MEM), Dulbecco's modified Eagle's medium (DMEM), RPMI1640 medium, 199 medium, F12 medium, and the like) and any of various buffers (for example, HEPES buffer, phosphate buffer, phosphate buffered saline, Tris-HCl buffer, borate buffer, acetate buffer, and the like).
  • a serum free medium suitable for fat cell differentiation of the cells for example, minimum essential medium (MEM), Dulbecco's modified Eagle's medium (DMEM), RPMI1640 medium, 199 medium, F12 medium, and the like
  • buffers for example, HEPES buffer, phosphate buffer, phosphate buffered saline, Tris-HCl buffer, borate buffer, acetate buffer, and the like.
  • the aforementioned medium may optionally contain blood serum (for example, about 5 to 20% of fetal bovine serum (FBS)), and a fat cell inducing aid (for example, isobutyl-methylxanthine (IBMX), dexamethasone, insulin, and the like) as required.
  • a fat cell inducing aid for example, isobutyl-methylxanthine (IBMX), dexamethasone, insulin, and the like
  • examples of other additives include transferrin, T3, cortisol, asc, calcium pantothenate, biotin, and the like.
  • a commercially available known kit for fat cell differentiation may also be used.
  • concentration of the test substance to be added should be changed depending on the type of the compound (solubility, toxicity, and the like), the concentration is appropriately chosen to be in the range of, for example, about 1 to 1000 ⁇ M, preferably about 5 to 500 ⁇ M, more preferably about 50 to 200 ⁇ M.
  • Time of the contact is, for example, about 1 to 48 hours, preferably about 5 to 36 hours, more preferably about 10 to 24 hours.
  • the cells may be cultured in a fat cell differentiation-inducing medium, while they are contacted with a test substance, or the cells may be contacted with a test substance for a certain period of time, and then cultured in a fat cell differentiation-inducing medium.
  • expression of an apoptosis-related gene is measured in the presence or absence of a test substance.
  • Expression of the PPAR ⁇ gene can be measured by the aforementioned method for measuring the PPAR ⁇ expression-inducing activity.
  • expressions of an apoptosis-related gene, a fat cell differentiation-related gene, and a lipid can also be measured by the aforementioned method for measuring the PPAR ⁇ -agonistic activity.
  • a prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or chondrosarcoma that can induce apoptosis or fat cell differentiation mediated by PPAR ⁇ in giant cell tumors occurring in a bone and soft tissue or in chondrosarcoma can be selected.
  • the test substance can be selected as a prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or for chondrosarcoma, which exhibits PPAR ⁇ -mediated efficacy thereof.
  • the test substance provides a statistically significant difference compared with the result obtained in the absence of the test substance, and a test substance that increases (or decreases) the expression amount of the PPAR ⁇ gene, an apoptosis-related gene, a fat cell differentiation-related gene, or a lipid by about 20% or more, preferably about 30% or more, more preferably about 50% or more, can be chosen as a prophylactic or therapeutic agent for giant cell tumors occurring in a bone and soft tissue or for chondrosarcoma.
  • Example 1 Analysis of suppression of cell proliferation and apoptosis of cultured cells of osteoclastoma (GCT) observed after addition of zaltoprofen
  • GCT cultured cells (case 1, patient with osteoclastoma in a distal part of the right femur, in twenties; case 2, patient with osteoclastoma in a distal part of the right femur, in twenties) were cultured on a 96-well culture plate, zaltoprofen was added to the cells at various concentrations (5, 10, 50, 100, and 200 ⁇ M), color development was attained with Cell Counting Kit-8 (CCK-8) (Dojindo) 24 hours thereafter, and absorbance was measured at 450 nm 3 hours thereafter ( Fig. 1 ). As a result, zaltoprofen concentration-dependent suppression of the cell proliferation was successfully observed.
  • the aforementioned GCT cultured cells of the case 1 were cultured on chamber cover slide glass, and zaltoprofen was added at different concentrations (100, and 200 ⁇ M) 24 hours afterward. Then, 8 hours and 24 hours afterward, the cells were fixed with 4% paraformaldehyde, staining with caspase 3 and Tunel assay were performed, and presence or absence of apoptosis was analyzed. Observation was performed with a fluorescence microscope (BZ-9000) of Keyence, and positive images for each concentration were quantitatively observed ( Figs. 2 to 5 ). As a result, zaltoprofen concentration and administration time-dependent increases of the Tunel-positive ratio and caspase 3-positive ratio were successfully observed.
  • Example 2 PPAR ⁇ immunostaining of cultured cells of osteoclastoma (GCT) performed after addition of zaltoprofen
  • the GCT cultured cells of the aforementioned case 1 were cultured on chamber cover slide glass, and 24 hours thereafter, zaltoprofen was added at various concentrations (10, 50, 100, and 200 ⁇ M). After 24 hours, the cells were fixed with 4% paraformaldehyde, and staining of PPAR ⁇ was performed. Observation was performed with a fluorescence microscope (BZ-9000) of Keyence, and positive images for each concentration were quantitatively observed ( Figs. 6 and 7 ). As a result, it was successfully observed that the expression of PPAR ⁇ was about 15% for the control, and the expression of PPAR ⁇ was increased in a zaltoprofen concentration-dependent manner.
  • Example 3 Analysis of fat cell differentiation of cultured cells of osteoclastoma (GCT) observed after addition of zaltoprofen
  • the GCT cultured cells of the aforementioned case 1 were cultured on chamber cover slide glass, and when they reached confluent, zaltoprofen was added to the cells at various concentrations (10, 50, and 100 ⁇ M). From 24 hours thereafter, the cells were cultured in a fat cell differentiation-inducing medium (STREMPRO Adipogenesis Differentiation Kit, Invitrogen) for 7 to 14 days, and differentiation into fat cells was analyzed with HCS LipidTOX Green Neutral Lipid Stain (Invitrogen) ( Figs. 8 and 9 ).
  • STREMPRO Adipogenesis Differentiation Kit Invitrogen
  • Example 4 Analysis of apoptosis of cells derived from patient with osteoclastoma (GCT) administered with zaltoprofen
  • Example 5 PPARy immunostaining of cells derived from patient with osteoclastoma (GCT) administered with zaltoprofen
  • Example 6 Analysis of suppression of cell proliferation of cultured cells of osteoclastoma (GCT) observed after addition of non-steroidal anti-inflammatory agent
  • Example 2 In the same manner as that of Example 1, the GCT cultured cells (case 1, case 2) were cultured, a non-steroidal anti-inflammatory agent (acetaminophen, indomethacin, or diclofenac) or troglitazone was added at various concentrations, and absorbance was measured at 450 nm ( Figs. 12 and 13 ). As a result, it was observed that the proliferation of cells was suppressed in a non-steroidal anti-inflammatory agent concentration-dependent manner.
  • acetaminophen, indomethacin, or diclofenac acetaminophen, indomethacin, or diclofenac
  • the cells (case 1, case 2) were cultured on a 96-well culture plate, allowed to react with PPAR ⁇ siRNA, negative control siRNA, or only with the transfection reagents (Thermo Scientific DharmaFECT, Thermo Scientific) for 48 hours, and further cultured in a usual culture medium for 48 hours. Then, 200 ⁇ M of zaltoprofen or 60 ⁇ M of troglitazone was added to the cells, 72 hours thereafter, color development was performed with Cell Counting Kit-8 (CCK-8, Dojindo), and 3 hours thereafter, absorbance was measured at 450 nm ( Figs. 14 and 15 ). As a result, it was observed that the effect of zaltoprofen was significantly suppressed in the PPAR ⁇ siRNA addition group.
  • Example 8 Analysis of suppression of cell proliferation and apoptosis of cells derived from giant cell tumor of tendon sheath (GCT of tendon sheath) or cells derived from pigmented villonodular synovitis (diffuse-type GCT) observed after addition of non-steroidal anti-inflammatory agent or thiazolidine derivative
  • Cultured cells of giant cell tumor of tendon sheath (patient with giant cell tumor of tendon sheath in the right knee, in 30's) and cultured cells of pigmented villonodular synovitis (patient with pigmented villonodular synovitis in the left knee, in 30's) were cultured in the same manner as that of Example 1, zaltoprofen or troglitazone was added to the cells at various concentrations, and absorbance was measured ( Figs. 16 and 17 ). As a result, it was observed that the cell proliferation was suppressed in a zaltoprofen or troglitazone concentration-dependent manner.
  • Example 2 the cultured cells of giant cell tumor of tendon sheath and the cultured cells of pigmented villonodular synovitis were subjected to staining with caspase 3 and Tunel assay, and presence or absence of apoptosis was analyzed ( Figs. 18 to 25 ). As a result, it was observed that the Tunel-positive ratio and caspase 3-positive ratio increased in the cells added with zaltoprofen at a concentration of 400 ⁇ M or troglitazone at a concentration of 200 ⁇ M compared with those observed for the control.
  • Example 9 PPARy immunostaining of cells derived from giant cell tumor of tendon sheath (GCT of tendon sheath) or cells derived from pigmented villonodular synovitis (diffuse-type GCT) performed after addition of non-steroidal anti-inflammatory agent or thiazolidine derivative
  • zaltoprofen or troglitazone was added at concentration of 400 ⁇ M or 200 ⁇ M, respectively, to the cells derived from giant cell tumor of tendon sheath or cells derived from pigmented villonodular synovitis, and PPAR ⁇ -positive images were observed ( Figs. 26 to 29 ).
  • PPAR ⁇ PPAR ⁇ -positive images were observed ( Figs. 26 to 29 ).
  • Example 10 Analysis of fat cell differentiation of cells derived from giant cell tumor of tendon sheath (GCT of tendon sheath) or cells derived from pigmented villonodular synovitis (diffuse-type GCT) observed after addition of non-steroidal anti-inflammatory agent
  • PPAR ⁇ is a transcription factor indispensable for fat cell differentiation. Therefore, zaltoprofen was added at a concentration of 400 ⁇ M to the cells derived from giant cell tumor of tendon sheath or the cells derived from pigmented villonodular synovitis, and differentiation into fat cells was analyzed ( Figs. 30 and 31 ). As a result, it was successfully observed that the positive images obtained with HCS LipidTOX Green Neutral Lipid Stain increased in the zaltoprofen-added cells compared with the control.
  • Example 11 Analysis of suppression of cell proliferation of cultured cells of osteoclastoma (GCT) observed after addition of pioglitazone
  • the GCT cultured cells (case 1, case 2), the cells derived from giant cell tumor of tendon sheath (GCT of tendon sheath), or the cells derived from pigmented villonodular synovitis (diffuse-type GCT) were cultured, and then pioglitazone, a thiazolidine derivative, was added at various concentrations, and absorbance was measured at 450 nm ( Fig. 32 ). As a result, it was observed that the proliferation of cells was suppressed in a pioglitazone concentration-dependent manner.
  • Example 12 Analysis of MRI image of patient with osteoclastoma (GCT), patient with giant cell tumor of tendon sheath, or patient with pigmented villonodular synovitis administered with zaltoprofen
  • Soleton Tablet 80 (generic name: zaltoprofen, 80 mg, Nippon Chemiphar) was administered to a patient with osteoclastoma, a patient with giant cell tumor of tendon sheath, or a patient with pigmented villonodular synovitis at a dose of 3 tablets per day (administered in morning, at noon, and in evening), and the 11 806 927 was evaluated by MRI every several months.
  • a typical case in a case of recurrence of osteoclastoma in the pelvic part (34 years old, female, Figs. 33 and 34 ), gradual shrinkage of the tumor was observed after two months ( Fig. 35 ) and four months ( Fig. 36 ).
  • Example 13 Analysis of suppression of cell proliferation and apoptosis of chondrosarcoma-derived cell line (H-EMC-SS) observed after addition of non-steroidal anti-inflammatory agent or thiazolidine derivative
  • Example 2 In the same manner as that of Example 1, the cell line derived from chondrosarcoma was cultured, troglitazone, pioglitazone, or zaltoprofen was added at various concentrations, and absorbance was measured ( Fig. 45 ). As a result, it was observed that the cell proliferation was suppressed in a troglitazone, pioglitazone, or zaltoprofen concentration-dependent manner.
  • the chondrosarcoma-derived cell line was subjected to caspase 3 staining, and presence or absence of apoptosis was analyzed ( Figs. 46 and 47 ).
  • the caspase 3-positive ratio increased in the cells added with zaltoprofen at a concentration of 200 ⁇ M, troglitazone at a concentration of 100 ⁇ M, or pioglitazone at a concentration of 200 ⁇ M, compared with the control.
  • Example 14 PPAR ⁇ immunostaining of chondrosarcoma-derived cell line (H-EMC-SS) performed after addition of non-steroidal anti-inflammatory agent or thiazolidine derivative
  • Example 2 In the same manner as that of Example 2, to the chondrosarcoma-derived cell line was added zaltoprofen at a concentration of 200 ⁇ M, troglitazone at a concentration of 100 ⁇ M, or pioglitazone at a concentration of 200 ⁇ M, and the PPAR ⁇ -positive images were measured ( Figs. 48 and 49 ). As a result, expression of PPAR ⁇ was successfully observed in the zaltoprofen, troglitazone, or pioglitazone-added cells.
  • the prophylactic or therapeutic agent of the present invention is effective for a patient with giant cell tumor occurring in a bone and soft tissue or with chondrosarcoma, or a person having a risk of onset of giant cell tumor occurring in a bone and soft tissue or that of chondrosarcoma. Further, according to the present invention, research of a novel therapeutic agent for giant cell tumors occurring in a bone and soft tissue or chondrosarcoma is achievable by selecting a test substance that controls the PPAR ⁇ gene and apoptosis, or fat cell differentiation.

Claims (4)

  1. Composition pharmaceutique comprenant du zaltoprofène pour une utilisation dans la prévention ou le traitement de tumeurs à cellules géantes survenant dans un os et du tissu mou ou d'un chondrosarcome.
  2. Composition pharmaceutique selon la revendication 1 pour une utilisation selon la revendication 1, dans laquelle une prolifération de tumeurs à cellules géantes survenant dans un os et du tissu mou ou d'un chondrosarcome est supprimée.
  3. Composition selon l'une quelconque des revendications 1 à 2 pour une utilisation selon l'une quelconque des revendications 1 à 2, dans laquelle la tumeur à cellules géantes survenant dans un os et du tissu mou est choisie dans le groupe comprenant un ostéoclastome, une tumeur à cellules géantes de gaine de tendon, et une synovite villonodulaire pigmentée.
  4. Composition selon l'une quelconque des revendications 1 à 3 pour une utilisation selon l'une quelconque des revendications 1 à 3, dans laquelle la taille de tumeur d'un ostéoclastome, d'une tumeur à cellules géantes de gaine de tendon, et d'une synovite villonodulaire pigmentée est diminuée.
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